oculocutaneous albinism 5 (autosomal recessive)

Preferred Label : oculocutaneous albinism 5 (autosomal recessive);

Obsolete resource : true;

Approved symbol HGNC : OCA5;

Chromosome HGNC : 4q24;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:44139;

UMLS CUI

C3809110;

Automatic exact mappings (from CISMeF team)
- Albinism, oculocutaneous, type V [OMIM Phenotype]
NCIt concept
- OCA5 Gene [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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